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Fredrik Mertens

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Trombetta Domenico; Mertens Fredrik; Lonoce Angelo; D'Addabbo Pietro; Rennstam Karin; Mandahl Nils; Storlazzi Clelia Tiziana
Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.
Brekke Helge R; Kolberg Matthias; Skotheim Rolf I; Hall Kirsten S; Bjerkehagen Bodil; Risberg Björn; Domanski Henryk A; Mandahl Nils; Liestøl Knut; Smeland Sigbjørn; Danielsen Håvard E; Mertens Fredrik; Lothe Ragnhild A
Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors.
Domanski H A; Mertens F; Panagopoulos I; Akerman M
Low-grade fibromyxoid sarcoma is difficult to diagnose by fine needle aspiration cytology: a cytomorphological study of eight cases.

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All Publications

2009: Trombetta Domenico; Mertens Fredrik; Lonoce Angelo; D'Addabbo Pietro; Rennstam Karin; Mandahl Nils; Storlazzi Clelia Tiziana
Characterization of a hotspot region on chromosome 12 for amplification in ring chromosomes in atypical lipomatous tumors.
Genes, chromosomes & cancer 2009;48(11):993-1001.
2009: Brekke Helge R; Kolberg Matthias; Skotheim Rolf I; Hall Kirsten S; Bjerkehagen Bodil; Risberg Björn; Domanski Henryk A; Mandahl Nils; Liestøl Knut; Smeland Sigbjørn; Danielsen Håvard E; Mertens Fredrik; Lothe Ragnhild A
Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors.
Neuro-oncology 2009;11(5):514-28.
2009: Domanski H A; Mertens F; Panagopoulos I; Akerman M
Low-grade fibromyxoid sarcoma is difficult to diagnose by fine needle aspiration cytology: a cytomorphological study of eight cases.
Cytopathology : official journal of the British Society for Clinical Cytology 2009;20(5):304-14.
2009: Mertens Fredrik; Antonescu Cristina R; Hohenberger Peter; Ladanyi Marc; Modena Piergiorgio; D'Incalci Maurizio; Casali Paolo G; Aglietta Massimo; Alvegård Thor
Translocation-related sarcomas.
Seminars in oncology 2009;36(4):312-23.
2009: Gorunova Ludmila; Vult von Steyern Fredrik; Storlazzi Clelia Tiziana; Bjerkehagen Bodil; Follerås Gunnar; Heim Sverre; Mandahl Nils; Mertens Fredrik
Cytogenetic analysis of 101 giant cell tumors of bone: nonrandom patterns of telomeric associations and other structural aberrations.
Genes, chromosomes & cancer 2009;48(7):583-602.
2009: Hallor Karolin H; Staaf Johan; Bovée Judith V M G; Hogendoorn Pancras C W; Cleton-Jansen Anne-Marie; Knuutila Sakari; Savola Suvi; Niini Tarja; Brosjö Otte; Bauer Henrik C F; Vult von Steyern Fredrik; Jonsson Kjell; Skorpil Mikael; Mandahl Nils; Mertens Fredrik
Genomic profiling of chondrosarcoma: chromosomal patterns in central and peripheral tumors.
Clinical cancer research : an official journal of the American Association for Cancer Research 2009;15(8):2685-94.
2009: Hallor Karolin H; Sciot Raf; Staaf Johan; Heidenblad Markus; Rydholm Anders; Bauer Henrik Cf; Aström Kristina; Domanski Henryk A; Meis Jeanne M; Kindblom Lars-Gunnar; Panagopoulos Ioannis; Mandahl Nils; Mertens Fredrik
Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.
The Journal of pathology 2009;217(5):716-27.
2009: Möller Emely; Mandahl Nils; Iliszko Mariola; Mertens Fredrik; Panagopoulos Ioannis
Bidirectionality and transcriptional activity of the EWSR1 promoter region.
Oncology reports 2009;21(3):641-8.
2009: Panagopoulos Ioannis; Mertens Fredrik
Characterization of the human CREB3L2 gene promoter.
Oncology reports 2009;21(3):615-24.
2009: Bartuma Hammurabi; Panagopoulos Ioannis; Collin Anna; Trombetta Domenico; Domanski Henryk A; Mandahl Nils; Mertens Fredrik
Expression levels of HMGA2 in adipocytic tumors correlate with morphologic and cytogenetic subgroups.
Molecular cancer 2009;8():36.
2009: Gebre-Medhin S; Broberg K; Jonson T; Gorunova L; von Steyern F Vult; Brosjö O; Jin Y; Gisselsson D; Panagopoulos I; Mandahl N; Mertens F
Telomeric associations correlate with telomere length reduction and clonal chromosome aberrations in giant cell tumor of bone.
Cytogenetic and genome research 2009;124(2):121-7.
2008: Panagopoulos Ioannis; Möller Emely; Collin Anna; Mertens Fredrik
The POU5F1P1 pseudogene encodes a putative protein similar to POU5F1 isoform 1.
Oncology reports 2008;20(5):1029-33.
2008: Stewénius Ylva; Jin Yuesheng; Ora Ingrid; Panagopoulos Ioannis; Möller Emely; Mertens Fredrik; Sandstedt Bengt; Alumets Jan; Akerman Måns; Merks Johannes Hm; de Kraker Jan; Gisselsson David
High-resolution molecular cytogenetic analysis of Wilms tumors highlights diagnostic difficulties among small round cell kidney tumors.
Genes, chromosomes & cancer 2008;47(10):845-52.
2008: Panagopoulos Ioannis; Mertens Fredrik; Griffin Constance A
An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera.
Cancer genetics and cytogenetics 2008;185(2):74-7.
2008: Panagopoulos Ioannis; Möller Emely; Isaksson Margareth; Mertens Fredrik
A PCR/restriction digestion assay for the detection of the transcript variants 1 and 2 of POU5F1.
Genes, chromosomes & cancer 2008;47(6):521-9.
2008: Bartuma Hammurabi; Domanski Henryk A; Von Steyern Fredrik Vult; Kullendorff Carl-Magnus; Mandahl Nils; Mertens Fredrik
Cytogenetic and molecular cytogenetic findings in lipoblastoma.
Cancer genetics and cytogenetics 2008;183(1):60-3.
2008: Möller E; Stenman G; Mandahl N; Hamberg H; Mölne L; van den Oord J J; Brosjö O; Mertens F; Panagopoulos I
POU5F1, encoding a key regulator of stem cell pluripotency, is fused to EWSR1 in hidradenoma of the skin and mucoepidermoid carcinoma of the salivary glands.
The Journal of pathology 2008;215(1):78-86.
2008: Strömberg Ulf; Björk Jonas; Broberg Karin; Mertens Fredrik; Vineis Paolo
Selection of influential genetic markers among a large number of candidates based on effect estimation rather than hypothesis testing: an approach for genome-wide association studies.
Epidemiology (Cambridge, Mass.) 2008;19(2):302-8.
2008: Jin Charlotte; Jin Yuesheng; Wennerberg Johan; Rosenquist Bo; Mertens Fredrik
Increased sensitivity to bleomycin in upper aerodigestive tract mucosa of head and neck squamous cell carcinoma patients.
Mutation research 2008;652(1):30-7.
2008: Hallor K H; Staaf J; Jönsson G; Heidenblad M; Vult von Steyern F; Bauer H C F; Ijszenga M; Hogendoorn P C W; Mandahl N; Szuhai K; Mertens F
Frequent deletion of the CDKN2A locus in chordoma: analysis of chromosomal imbalances using array comparative genomic hybridisation.
British journal of cancer 2008;98(2):434-42.
2008: Panagopoulos Ioannis; Mertens Fredrik; Löfvenberg Richard; Mandahl Nils
Fusion of the COL1A1 and USP6 genes in a benign bone tumor.
Cancer genetics and cytogenetics 2008;180(1):70-3.
2008: Möller Emely; Mandahl Nils; Mertens Fredrik; Panagopoulos Ioannis
Molecular identification of COL6A3-CSF1 fusion transcripts in tenosynovial giant cell tumors.
Genes, chromosomes & cancer 2008;47(1):21-5.
2007: Lindberg Eva; Persson Annette; Øra Ingrid; Mertens Fredrik; Englund Elisabet; Gisselsson David
Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma.
Neuropathology : official journal of the Japanese Society of Neuropathology 2007;27(6):556-60.
2007: Mertens Fredrik; Wiebe Thomas; Adlercreutz Catharina; Mandahl Nils; French Christopher A
Successful treatment of a child with t(15;19)-positive tumor.
Pediatric blood & cancer 2007;49(7):1015-7.
2007: Möller Emely; Isaksson Margareth; Mandahl Nils; Mertens Fredrik; Panagopoulos Ioannis
Comparison of the proximal promoter regions of the PAX3 and PAX7 genes.
Cancer genetics and cytogenetics 2007;178(2):114-9.
2007: Johnsson Anna; Collin Anna; Rydholm Anders; Domanski Henryk A; Mertens Fredrik; Mandahl Nils
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
Cancer genetics and cytogenetics 2007;177(1):59-63.
2007: Glanz C; Rebetz J; Stewénius Y; Persson A; Englund E; Mandahl N; Mertens F; Salford L G; Widegren B; Fan X; Gisselsson D
Genetic intratumour heterogeneity in high-grade brain tumours is associated with telomere-dependent mitotic instability.
Neuropathology and applied neurobiology 2007;33(4):440-54.
2007: Bartuma Hammurabi; Hallor Karolin H; Panagopoulos Ioannis; Collin Anna; Rydholm Anders; Gustafson Pelle; Bauer Henrik C F; Brosjö Otte; Domanski Henryk A; Mandahl Nils; Mertens Fredrik
Assessment of the clinical and molecular impact of different cytogenetic subgroups in a series of 272 lipomas with abnormal karyotype.
Genes, chromosomes & cancer 2007;46(6):594-606.
2007: Hallor Karolin H; Micci Francesca; Meis-Kindblom Jeanne M; Kindblom Lars-Gunnar; Bacchini Patrizia; Mandahl Nils; Mertens Fredrik; Panagopoulos Ioannis
Fusion genes in angiomatoid fibrous histiocytoma.
Cancer letters 2007;251(1):158-63.
2007: Soller Maria Johansson; Kullendorff Carl-Magnus; Békássy Albert N; Alumets Jan; Mertens Fredrik
Cytogenetic findings in pediatric renal cell carcinoma.
Cancer genetics and cytogenetics 2007;173(1):75-80.
2007: Panagopoulos Ioannis; Möller Emely; Dahlén Anna; Isaksson Margareth; Mandahl Nils; Vlamis-Gardikas Alexios; Mertens Fredrik
Characterization of the native CREB3L2 transcription factor and the FUS/CREB3L2 chimera.
Genes, chromosomes & cancer 2007;46(2):181-91.
2007: Hallor Karolin H; Heidenblad Markus; Brosjö Otte; Mandahl Nils; Mertens Fredrik
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
Cancer genetics and cytogenetics 2007;172(1):80-3.
2006: Heidenblad M; Hallor K H; Staaf J; Jönsson G; Borg A; Höglund M; Mertens F; Mandahl N
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
Oncogene 2006;25(53):7106-16.
2006: Storlazzi C T; Brekke H R; Mandahl N; Brosjö O; Smeland S; Lothe R A; Mertens F
Identification of a novel amplicon at distal 17q containing the BIRC5/SURVIVIN gene in malignant peripheral nerve sheath tumours.
The Journal of pathology 2006;209(4):492-500.
2006: Domanski Henryk A; Akerman Måns; Engellau Jacob; Gustafson Pelle; Mertens Fredrik; Rydholm Anders
Fine-needle aspiration of neurilemoma (schwannoma). A clinicocytopathologic study of 116 patients.
Diagnostic cytopathology 2006;34(6):403-12.
2006: Jin Yuesheng; Mertens Fredrik; Kullendorff Carl-Magnus; Panagopoulos Ioannis
Fusion of the tumor-suppressor gene CHEK2 and the gene for the regulatory subunit B of protein phosphatase 2 PPP2R2A in childhood teratoma.
Neoplasia (New York, N.Y.) 2006;8(5):413-8.
2006: Storlazzi Clelia Tiziana; Wozniak Agnieszka; Panagopoulos Ioannis; Sciot Raf; Mandahl Nils; Mertens Fredrik; Debiec-Rychter Maria
Rearrangement of the COL12A1 and COL4A5 genes in subungual exostosis: molecular cytogenetic delineation of the tumor-specific translocation t(X;6)(q13-14;q22).
International journal of cancer. Journal international du cancer 2006;118(8):1972-6.
2006: Panagopoulos Ioannis; Nilsson Therese; Domanski Henryk A; Isaksson Margareth; Lindblom Pia; Mertens Fredrik; Mandahl Nils
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor.
International journal of cancer. Journal international du cancer 2006;118(5):1181-6.
2006: Jin Charlotte; Jin Yuesheng; Wennerberg Johan; Annertz Karin; Enoksson Jens; Mertens Fredrik
Cytogenetic abnormalities in 106 oral squamous cell carcinomas.
Cancer genetics and cytogenetics 2006;164(1):44-53.
2006: Mertens Fredrik; Strömberg Ulf; Rydholm Anders; Gustafson Pelle; Bauer Henrik C F; Brosjö Otte; Mandahl Nils
Prognostic significance of chromosome aberrations in high-grade soft tissue sarcomas.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2006;24(2):315-20.
2006: Jin C; Jin Y; Gisselsson D; Wennerberg J; Wah T S; Strömbäck B; Kwong Y-L; Mertens F
Molecular cytogenetic characterization of the 11q13 amplicon in head and neck squamous cell carcinoma.
Cytogenetic and genome research 2006;115(2):99-106.
2006: Schaad K; Strömbeck B; Mandahl N; Andersen M K; Heim S; Mertens F; Johansson B
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2).
Cytogenetic and genome research 2006;114(2):126-30.
2006: Nilsson M; Mertens F; Höglund M; Mandahl N; Panagopoulos I
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
Cytogenetic and genome research 2006;112(1-2):60-6.
2005: Storlazzi Clelia Tiziana; Von Steyern Fredrik Vult; Domanski Henryk A; Mandahl Nils; Mertens Fredrik
Biallelic somatic inactivation of the NF1 gene through chromosomal translocations in a sporadic neurofibroma.
International journal of cancer. Journal international du cancer 2005;117(6):1055-7.
2005: Nilsson M; Panagopoulos I; Mertens F; Mandahl N
Fusion of the HMGA2 and NFIB genes in lipoma.
Virchows Archiv : an international journal of pathology 2005;447(5):855-8.
2005: Surace Cecilia; Storlazzi Clelia Tiziana; Engellau Jacob; Domanski Henryk A; Gustafson Pelle; Panagopoulos Ioannis; D'Addabbo Pietro; Rocchi Mariano; Mandahl Nils; Mertens Fredrik
Molecular cytogenetic characterization of an ins(4;X) occurring as the sole abnormality in an aggressive, poorly differentiated soft tissue sarcoma.
Virchows Archiv : an international journal of pathology 2005;447(5):869-74.
2005: Hallor Karolin Hansén; Mertens Fredrik; Jin Yuesheng; Meis-Kindblom Jeanne M; Kindblom Lars-Gunnar; Behrendtz Mikael; Kalén Anders; Mandahl Nils; Panagopoulos Ioannis
Fusion of the EWSR1 and ATF1 genes without expression of the MITF-M transcript in angiomatoid fibrous histiocytoma.
Genes, chromosomes & cancer 2005;44(1):97-102.
2005: Domanski Henryk A; Akerman Måns; Carlén Birgitta; Engellau Jacob; Gustafson Pelle; Jonsson Kjell; Mertens Fredrik; Rydholm Anders
Core-needle biopsy performed by the cytopathologist: a technique to complement fine-needle aspiration of soft tissue and bone lesions.
Cancer 2005;105(4):229-39.
2005: Mitelman Felix; Mertens Fredrik; Johansson Bertil
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
Genes, chromosomes & cancer 2005;43(4):350-66.
2005: Stewénius Ylva; Gorunova Ludmila; Jonson Tord; Larsson Nina; Höglund Mattias; Mandahl Nils; Mertens Fredrik; Mitelman Felix; Gisselsson David
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(15):5541-6.
2005: Nilsson Malin; Domanski Henryk; Mertens Fredrik; Mandahl Nils
Atypical lipomatous tumor with rare structural rearrangements involving chromosomes 8 and 12.
Oncology reports 2005;13(4):649-52.
2005: Mertens Fredrik; Fletcher Christopher D M; Antonescu Cristina R; Coindre Jean-Michel; Colecchia Maurizio; Domanski Henryk A; Downs-Kelly Erinn; Fisher Cyril; Goldblum John R; Guillou Louis; Reid Robin; Rosai Juan; Sciot Raf; Mandahl Nils; Panagopoulos Ioannis
Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene.
Laboratory investigation; a journal of technical methods and pathology 2005;85(3):408-15.
2005: Panagopoulos Ioannis; Mertens Fredrik; Isaksson Margareth; Mandahl Nils
Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses).
Cancer genetics and cytogenetics 2005;156(1):74-6.
2004: Dahlén Anna; Mertens Fredrik; Mandahl Nils; Panagopoulos Ioannis
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
Biochemical and biophysical research communications 2004;325(4):1318-23.
2004: Nilsson Malin; Domanski Henryk A; Mertens Fredrik; Mandahl Nils
Molecular cytogenetic characterization of recurrent translocation breakpoints in bizarre parosteal osteochondromatous proliferation (Nora's lesion).
Human pathology 2004;35(9):1063-9.
2004: Surace Cecilia; Panagopoulos Ioannis; Pålsson Eva; Rocchi Mariano; Mandahl Nils; Mertens Fredrik
A novel FISH assay for SS18-SSX fusion type in synovial sarcoma.
Laboratory investigation; a journal of technical methods and pathology 2004;84(9):1185-92.
2004: Panagopoulos Ioannis; Mertens Fredrik; Isaksson Margareth; Mandahl Nils
Expression of DOL54 is not restricted to myxoid liposarcomas with the FUS-DDIT3 chimera but is found in various sarcomas.
Oncology reports 2004;12(1):107-10.
2004: Panagopoulos Ioannis; Storlazzi Clelia Tiziana; Fletcher Christopher D M; Fletcher Jonathan A; Nascimento Antonio; Domanski Henryk A; Wejde Johan; Brosjö Otte; Rydholm Anders; Isaksson Margareth; Mandahl Nils; Mertens Fredrik
The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.
Genes, chromosomes & cancer 2004;40(3):218-28.
2004: Kuzniacka Alina; Mertens Fredrik; Strömbeck Bodil; Wiegant Joop; Mandahl Nils
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma.
Cancer genetics and cytogenetics 2004;151(2):178-81.
2004: Dahlén Anna; Fletcher Christopher D M; Mertens Fredrik; Fletcher Jonathan A; Perez-Atayde Antonio R; Hicks M John; Debiec-Rychter Maria; Sciot Raf; Wejde Johan; Wedin Rikard; Mandahl Nils; Panagopoulos Ioannis
Activation of the GLI oncogene through fusion with the beta-actin gene (ACTB) in a group of distinctive pericytic neoplasms: pericytoma with t(7;12).
The American journal of pathology 2004;164(5):1645-53.
2004: Mandahl N; Mertens F; Panagopoulos I; Knuutila S
Genetic characterization of bone and soft tissue tumors.
Acta orthopaedica Scandinavica. Supplementum 2004;75(311):21-8.
2004: Mitelman Felix; Johansson Bertil; Mertens Fredrik
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer.
Nature genetics 2004;36(4):331-4.
2004: Höglund Mattias; Jin Charlotte; Gisselsson David; Hansen Gunnar B; Mitelman Felix; Mertens Fredrik
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
Cancer genetics and cytogenetics 2004;150(1):1-8.
2004: Nilsson Malin; Meza-Zepeda Leonardo A; Mertens Fredrik; Forus Anne; Myklebost Ola; Mandahl Nils
Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas.
International journal of cancer. Journal international du cancer 2004;109(3):363-9.
2004: Gisselsson David; Pålsson Eva; Yu Christina; Mertens Fredrik; Mandahl Nils
Mitotic instability associated with late genomic changes in bone and soft tissue tumours.
Cancer letters 2004;206(1):69-76.
2004: Johansson Bertil; Mertens Fredrik; Mitelman Felix
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia.
Annals of medicine 2004;36(7):492-503.
2004: Mertens F; Panagopoulos I; Jonson T; Gisselsson D; Isaksson M; Domanski H A; Mandahl N
Retained heterodisomy for chromosome 12 in atypical lipomatous tumors: implications for ring chromosome formation.
Cytogenetic and genome research 2004;106(1):33-8.
2003: Skotheim Rolf I; Kallioniemi Anne; Bjerkhagen Bodil; Mertens Fredrik; Brekke Helge R; Monni Outi; Mousses Spyro; Mandahl Nils; Soeter Gunnar; Nesland Jahn M; Smeland Sigbjørn; Kallioniemi Olli-P; Lothe Ragnhild A
Topoisomerase-II alpha is upregulated in malignant peripheral nerve sheath tumors and associated with clinical outcome.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2003;21(24):4586-91.
2003: Dahlén Anna; Mertens Fredrik; Rydholm Anders; Brosjö Otte; Wejde Johan; Mandahl Nils; Panagopoulos Ioannis
Fusion, disruption, and expression of HMGA2 in bone and soft tissue chondromas.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2003;16(11):1132-40.
2003: Adeyinka Adewale; Baldetorp Bo; Mertens Fredrik; Olsson Håkan; Johannsson Oskar; Heim Sverre; Pandis Nikos
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas.
Cancer genetics and cytogenetics 2003;147(1):62-7.
2003: Domanski Henryk A; Carlén Birgitta; Mertens Fredrik; Akerman Måns
Extraskeletal myxoid chondrosarcoma with neuroendocrine differentiation: a case report with fine-needle aspiration biopsy, histopathology, electron microscopy, and cytogenetics.
Ultrastructural pathology 2003;27(5):363-8.
2003: Storlazzi Clelia Tiziana; Mertens Fredrik; Nascimento Antonio; Isaksson Margareth; Wejde Johan; Brosjo Otte; Mandahl Nils; Panagopoulos Ioannis
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma.
Human molecular genetics 2003;12(18):2349-58.
2003: Storlazzi Clelia Tiziana; Mertens Fredrik; Domanski Henryk; Fletcher Christopher D M; Wiegant Joop; Mandahl Nils
Ring chromosomes and low-grade gene amplification in an atypical lipomatous tumor with minimal nuclear atypia.
International journal of oncology 2003;23(1):67-71.
2003: Storlazzi Clelia Tiziana; Mertens Fredrik; Mandahl Nils; Gisselsson David; Isaksson Margareth; Gustafson Pelle; Domanski Henryk A; Panagopoulos Ioannis
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma.
Genes, chromosomes & cancer 2003;37(2):195-200.
2003: Dahlén Anna; Debiec-Rychter Maria; Pedeutour Florence; Domanski Henryk A; Höglund Mattias; Bauer Henrik C F; Rydholm Anders; Sciot Raf; Mandahl Nils; Mertens Fredrik
Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors.
International journal of cancer. Journal international du cancer 2003;103(5):616-23.
2003: Kullendorff Carl Magnus; Soller Maria; Wiebe Thomas; Mertens Fredrik
Cytogenetic findings and clinical course in a consecutive series of Wilms tumors.
Cancer genetics and cytogenetics 2003;140(1):82-7.
2002: Panagopoulos Ioannis; Mertens Fredrik; Isaksson Margareth; Domanski Henryk A; Brosjö Otte; Heim Sverre; Bjerkehagen Bodil; Sciot Raf; Dal Cin Paola; Fletcher Jonathan A; Fletcher Christopher D M; Mandahl Nils
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
Genes, chromosomes & cancer 2002;35(4):340-52.
2002: Nilsson M; Höglund M; Panagopoulos I; Sciot R; Dal Cin P; Debiec-Rychter M; Mertens F; Mandahl N
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.
Virchows Archiv : an international journal of pathology 2002;441(5):475-80.
2002: Broberg Karin; Zhang Miao; Strömbeck Bodil; Isaksson Margareth; Nilsson Malin; Mertens Fredrik; Mandahl Nils; Panagopoulos Ioannis
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.
International journal of oncology 2002;21(2):321-6.
2002: Mertens Fredrik; Strömberg Ulf; Mandahl Nils; Dal Cin Paola; De Wever Ivo; Fletcher Christopher D M; Mitelman Felix; Rosai Juan; Rydholm Anders; Sciot Raf; Tallini Giovanni; Van Den Berghe Herman; Vanni Roberta; Willén Helena
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
Cancer research 2002;62(14):3980-4.
2002: Gisselsson D; Jonson T; Yu C; Martins C; Mandahl N; Wiegant J; Jin Y; Mertens F; Jin C
Centrosomal abnormalities, multipolar mitoses, and chromosomal instability in head and neck tumours with dysfunctional telomeres.
British journal of cancer 2002;87(2):202-7.
2002: Panagopoulos Ioannis; Mertens Fredrik; Dêbiec-Rychter Maria; Isaksson Margareth; Limon Janusz; Kardas Iwona; Domanski Henryk A; Sciot Raf; Perek Danuta; Crnalic Sead; Larsson Olle; Mandahl Nils
Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.
International journal of cancer. Journal international du cancer 2002;99(4):560-7.
2002: Jin Yuesheng; Jin Charlotte; Wennerberg Johan; Höglund Mattias; Mertens Fredrik
Cyclin D1 amplification in chromosomal band 11q13 is associated with overrepresentation of 3q21-q29 in head and neck carcinomas.
International journal of cancer. Journal international du cancer 2002;98(3):475-9.
2002: Mandahl Nils; Gustafson Pelle; Mertens Fredrik; Akerman Måns; Baldetorp Bo; Gisselsson David; Knuutila Sakari; Bauer Henrik C F; Larsson Olle
Cytogenetic aberrations and their prognostic impact in chondrosarcoma.
Genes, chromosomes & cancer 2002;33(2):188-200.
2002: Gisselsson David; Pålsson Eva; Höglund Mattias; Domanski Henryk; Mertens Fredrik; Pandis Nikos; Sciot Raf; Dal Cin Paola; Bridge Julia A; Mandahl Nils
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
Genes, chromosomes & cancer 2002;33(2):133-40.
2002: Jin Charlotte; Jin Yuesheng; Wennerberg Johan; Akervall Jan; Dictor Michael; Mertens Fredrik
Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck.
Cancer genetics and cytogenetics 2002;132(2):85-96.
2002: Akervall Jan; Borg Ake; Dictor Michael; Jin Charlotte; Jin Yuesheng; Tanner Minna; Isola Jorma; Mertens Fredrik; Wennerberg Johan
Chromosomal translocations involving 11q13 contribute to cyclin D1 overexpression in squamous cell carcinoma of the head and neck.
International journal of oncology 2002;20(1):45-52.
2001: Domanski H A; Carlén B; Jonsson K; Mertens F; Akerman M
Distinct cytologic features of spindle cell lipoma. A cytologic-histologic study with clinical, radiologic, electron microscopic, and cytogenetic correlations.
Cancer 2001;93(6):381-9.
2001: Dahlén A; Broberg K; Domanski H A; Toksvig-Larsen S; Lindstrand A; Mandahl N; Mertens F
Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis.
Cancer genetics and cytogenetics 2001;131(1):19-24.
2001: Gisselsson D; Jonson T; Petersén A; Strömbeck B; Dal Cin P; Höglund M; Mitelman F; Mertens F; Mandahl N
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(22):12683-8.
2001: Jin Y; Jin C; Wennerberg J; Höglund M; Mertens F
Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas.
Cancer genetics and cytogenetics 2001;130(2):111-7.
2001: Eriksson L; Mertens F; Akerman M; Wiegant J
Calcium pyrophosphate dihydrate crystal deposition disease in the temporomandibular joint: diagnostic difficulties and clonal chromosome aberrations in a case followed up for 5 years.
Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons 2001;59(10):1217-20.
2001: Panagopoulos I; Mertens F; Domanski H A; Isaksson M; Brosjö O; Gustafson P; Mandahl N
No EWS/FLI1 fusion transcripts in giant-cell tumors of bone.
International journal of cancer. Journal international du cancer 2001;93(6):769-72.
2001: Panagopoulos I; Mertens F; Isaksson M; Limon J; Gustafson P; Skytting B; Akerman M; Sciot R; Dal Cin P; Samson I; Iliszko M; Ryoe J; Dêbiec-Rychter M; Szadowska A; Brosjö O; Larsson O; Rydholm A; Mandahl N
Clinical impact of molecular and cytogenetic findings in synovial sarcoma.
Genes, chromosomes & cancer 2001;31(4):362-72.
2001: Höglund M; Gisselsson D; Mandahl N; Johansson B; Mertens F; Mitelman F; Säll T
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution.
Genes, chromosomes & cancer 2001;31(2):156-71.
2001: Broberg K; Tallini G; Höglund M; Lindstrand A; Toksvig-Larsen S; Mertens F
The tumor-associated gene HMGIC is expressed in normal and osteoarthritis-affected synovia.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2001;14(4):311-7.
2001: Broberg K; Toksvig-Larsen S; Lindstrand A; Mertens F
Trisomy 7 accumulates with age in solid tumors and non-neoplastic synovia.
Genes, chromosomes & cancer 2001;30(3):310-5.
2001: Lothe R A; Smith-Sørensen B; Hektoen M; Stenwig A E; Mandahl N; Saeter G; Mertens F
Biallelic inactivation of TP53 rarely contributes to the development of malignant peripheral nerve sheath tumors.
Genes, chromosomes & cancer 2001;30(2):202-6.
2001: Jin C; Martins C; Jin Y; Wiegant J; Wennerberg J; Dictor M; Gisselsson D; Strömbeck B; Fonseca I; Mitelman F; Tanke H J; Höglund M; Mertens F
Characterization of chromosome aberrations in salivary gland tumors by FISH, including multicolor COBRA-FISH.
Genes, chromosomes & cancer 2001;30(2):161-7.
2001: Gisselsson D; Björk J; Höglund M; Mertens F; Dal Cin P; Akerman M; Mandahl N
Abnormal nuclear shape in solid tumors reflects mitotic instability.
The American journal of pathology 2001;158(1):199-206.
2000: Panagopoulos I; Mertens F; Isaksson M; Mandahl N
A novel FUS/CHOP chimera in myxoid liposarcoma.
Biochemical and biophysical research communications 2000;279(3):838-45.
2000: Jin Y; Jin C; Salemark L; Martins C; Wennerberg J; Mertens F
Centromere cleavage is a mechanism underlying isochromosome formation in skin and head and neck carcinomas.
Chromosoma 2000;109(7):476-81.
2000: Gisselsson D; Pettersson L; Höglund M; Heidenblad M; Gorunova L; Wiegant J; Mertens F; Dal Cin P; Mitelman F; Mandahl N
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(10):5357-62.
2000: Jin C; Jin Y; Wennerberg J; Dictor M; Mertens F
Nonrandom pattern of cytogenetic abnormalities in squamous cell carcinoma of the larynx.
Genes, chromosomes & cancer 2000;28(1):66-76.
2000: Adeyinka A; Mertens F; Bondeson L; Garne J P; Borg A; Baldetorp B; Pandis N
Cytogenetic heterogeneity and clonal evolution in synchronous bilateral breast carcinomas and their lymph node metastases from a male patient without any detectable BRCA2 germline mutation.
Cancer genetics and cytogenetics 2000;118(1):42-7.
2000: Parada L A; Limon J; Iliszko M; Czauderna P; Gisselsson D; Höglund M; Kullendorff C M; Wiebe T; Mertens F; Johansson B
Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study.
Medical and pediatric oncology 2000;34(3):165-70.
2000: Adeyinka A; Kytola S; Mertens F; Pandis N; Larsson C
Spectral karyotyping and chromosome banding studies of primary breast carcinomas and their lymph node metastases.
International journal of molecular medicine 2000;5(3):235-40.
2000: Mertens F; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; van Den Berghe H; Vanni R; Willén H
Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group.
The Journal of pathology 2000;190(1):31-8.
2000: Mertens F; Larramendy M; Gustavsson A; Gisselsson D; Rydholm A; Brosjö O; Mitelman F; Knuutila S; Mandahl N
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p.
Cancer genetics and cytogenetics 2000;116(2):89-96.
2000: Mandahl N; Fletcher C D; Dal Cin P; De Wever I; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van Den Berghe H; Vanni R; Willén H
Comparative cytogenetic study of spindle cell and pleomorphic leiomyosarcomas of soft tissues: a report from the CHAMP Study Group.
Cancer genetics and cytogenetics 2000;116(1):66-73.
2000: Akervall J; Wennerberg J; Mertens F
Chromosomal abnormalities in squamous cell carcinoma of the head and neck.
Advances in oto-rhino-laryngology 2000;56():261-7.
1999: Panagopoulos I; Mencinger M; Dietrich C U; Bjerkehagen B; Saeter G; Mertens F; Mandahl N; Heim S
Fusion of the RBP56 and CHN genes in extraskeletal myxoid chondrosarcomas with translocation t(9;17)(q22;q11).
Oncogene 1999;18(52):7594-8.
1999: Gisselsson D; Domanski H A; Höglund M; Carlén B; Mertens F; Willén H; Mandahl N
Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics.
The American journal of surgical pathology 1999;23(10):1300-4.
1999: Berner J M; Sørlie T; Mertens F; Henriksen J; Saeter G; Mandahl N; Brøgger A; Myklebost O; Lothe R A
Chromosome band 9p21 is frequently altered in malignant peripheral nerve sheath tumors: studies of CDKN2A and other genes of the pRB pathway.
Genes, chromosomes & cancer 1999;26(2):151-60.
1999: Gisselsson D; Höglund M; Mertens F; Mandahl N
Variable stability of chromosomes containing amplified alpha-satellite sequences in human mesenchymal tumours.
Chromosoma 1999;108(5):271-7.
1999: Adeyinka A; Mertens F; Idvall I; Bondeson L; Ingvar C; Mitelman F; Pandis N
Different patterns of chromosomal imbalances in metastasising and non-metastasising primary breast carcinomas.
International journal of cancer. Journal international du cancer 1999;84(4):370-5.
1999: Dictor M; Ehinger M; Mertens F; Akervall J; Wennerberg J
Abnormal cell cycle regulation in malignancy.
American journal of clinical pathology 1999;112(1 Suppl 1):S40-52.
1999: Mandahl N; Mertens F; Mitelman F
Genetic changes in bone and soft tissue tumors.
Acta orthopaedica Scandinavica. Supplementum 1999;285():30-40.
1999: Adeyinka A; Mertens F; Idvall I; Bondeson L; Pandis N
Multiple polysomies in breast carcinomas: preferential gain of chromosomes 1, 5, 6, 7, 12, 16, 17, 18, and 19.
Cancer genetics and cytogenetics 1999;111(2):144-8.
1999: Persson K; Pandis N; Mertens F; Borg A; Baldetorp B; Killander D; Isola J
Chromosomal aberrations in breast cancer: a comparison between cytogenetics and comparative genomic hybridization.
Genes, chromosomes & cancer 1999;25(2):115-22.
1999: Gisselsson D; Höglund M; Mertens F; Johansson B; Dal Cin P; Van den Berghe H; Earnshaw W C; Mitelman F; Mandahl N
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells.
Human genetics 1999;104(4):315-25.
1999: Broberg K; Höglund M; Limon J; Lindstrand A; Toksvig-Larsen S; Mandahl N; Mertens F
Rearrangement of the neoplasia-associated gene HMGIC in synovia from patients with osteoarthritis.
Genes, chromosomes & cancer 1999;24(3):278-82.
1999: Martins C; Jin Y; Jin C; Wennerberg J; Höglund M; Mertens F
Fluorescent in situ hybridisation (FISH) characterisation of pericentromeric breakpoints on chromosome 5 in head and neck squamous cell carcinomas.
European journal of cancer (Oxford, England : 1990) 1999;35(3):498-501.
1999: Kullendorff C M; Mertens F; Donnér M; Wiebe T; Akerman M; Mandahl N
Cytogenetic aberrations in Ewing sarcoma: are secondary changes associated with clinical outcome?
Medical and pediatric oncology 1999;32(2):79-83.
1998: Jin Y; Jin C; Wennerberg J; Mertens F; Höglund M
Cytogenetic and fluorescence in situ hybridization characterization of chromosome 1 rearrangements in head and neck carcinomas delineate a target region for deletions within 1p11-1p13.
Cancer research 1998;58(24):5859-65.
1998: Lundin C P; Mertens F; Rizou H; Idvall I; Georgiou G; Ingvar C; Pandis N
Cytogenetic changes in benign proliferative and nonproliferative lesions of the breast.
Cancer genetics and cytogenetics 1998;107(2):118-20.
1998: Gisselsson D; Andreasson P; Meis-Kindblom J M; Kindblom L G; Mertens F; Mandahl N
Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma.
Cancer genetics and cytogenetics 1998;107(2):102-6.
1998: Gisselsson D; Höglund M; O'Brien K P; Dumanski J P; Mertens F; Mandahl N
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences.
Cancer letters 1998;133(2):129-34.
1998: Gisselsson D; Höglund M; Mertens F; Mitelman F; Mandahl N
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization.
Genes, chromosomes & cancer 1998;23(3):203-12.
1998: Lundin C P; Mertens F; Ingvar C; Idvall I; Pandis N
Trisomy 16 as the primary chromosome aberration in a papilloma of the breast.
Cancer genetics and cytogenetics 1998;106(1):90-1.
1998: Mertens F; Kullendorff C M; Moëll C; Alumets J; Mandahl N
Complex karyotype in a childhood adrenocortical carcinoma.
Cancer genetics and cytogenetics 1998;105(2):190-2.
1998: Jin C; Jin Y; Höglund M; Wennerberg J; Akervall J; Willén R; Dictor M; Mandahl N; Mitelman F; Mertens F
Cytogenetic and molecular genetic demonstration of polyclonality in an acinic cell carcinoma.
British journal of cancer 1998;78(3):292-5.
1998: Adeyinka A; Mertens F; Idvall I; Bondeson L; Ingvar C; Heim S; Mitelman F; Pandis N
Cytogenetic findings in invasive breast carcinomas with prognostically favourable histology: a less complex karyotypic pattern?
International journal of cancer. Journal international du cancer 1998;79(4):361-4.
1998: Jin Y; Höglund M; Jin C; Martins C; Wennerberg J; Akervall J; Mandahl N; Mitelman F; Mertens F
FISH characterization of head and neck carcinomas reveals that amplification of band 11q13 is associated with deletion of distal 11q.
Genes, chromosomes & cancer 1998;22(4):312-20.
1998: Pandis N; Teixeira M R; Adeyinka A; Rizou H; Bardi G; Mertens F; Andersen J A; Bondeson L; Sfikas K; Qvist H; Apostolikas N; Mitelman F; Heim S
Cytogenetic comparison of primary tumors and lymph node metastases in breast cancer patients.
Genes, chromosomes & cancer 1998;22(2):122-9.
1998: Jin Y; Mertens F; Persson B; Warloe T; Gullestad H P; Salemark L; Jin C; Jonsson N; Risberg B; Mandahl N; Mitelman F; Heim S
Nonrandom numerical chromosome abnormalities in basal cell carcinomas.
Cancer genetics and cytogenetics 1998;103(1):35-42.
1998: Mandahl N; Mertens F; Willén H; Rydholm A; Kreicbergs A; Mitelman F
Nonrandom pattern of telomeric associations in atypical lipomatous tumors with ring and giant marker chromosomes.
Cancer genetics and cytogenetics 1998;103(1):25-34.
1998: Mertens F; Fletcher C D; Dal Cin P; De Wever I; Mandahl N; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Vanni R; Willén H
Cytogenetic analysis of 46 pleomorphic soft tissue sarcomas and correlation with morphologic and clinical features: a report of the CHAMP Study Group. Chromosomes and MorPhology.
Genes, chromosomes & cancer 1998;22(1):16-25.
1998: Akervall J; Jin Y; Baldetorp B; Mertens F; Wennerberg J
Complex karyotypes in flow cytometrically DNA-diploid squamous cell carcinomas of the head and neck.
British journal of cancer 1998;77(7):1082-8.
1998: Jin Y; Jin C; Mertens F; Persson B; Jonsson N
Characterization of a malignant eccrine poroma by cytogenetic and fluorescence in situ hybridization techniques.
Cancer genetics and cytogenetics 1998;102(2):100-3.
1998: Mertens F; Kullendorff C M; Hjorth L; Alumets J; Mandahl N
Trisomy 3 as the sole karyotypic change in a pediatric immature teratoma.
Cancer genetics and cytogenetics 1998;102(1):83-5.
1998: Jin Y; Jin C; Arheden K; Larsson O; Bauer H F; Mandahl N; Mertens F
Unbalanced chromosomal rearrangements in a metastasizing salivary gland tumor with benign histology.
Cancer genetics and cytogenetics 1998;102(1):59-64.
1998: Willén H; Akerman M; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Vanni R
Comparison of chromosomal patterns with clinical features in 165 lipomas: a report of the CHAMP study group.
Cancer genetics and cytogenetics 1998;102(1):46-9.
1998: Kullendorff C M; Donner M; Mertens F; Mandahl N
Chromosomal aberrations in a consecutive series of childhood rhabdomyosarcoma.
Medical and pediatric oncology 1998;30(3):156-9.
1998: Schuborg C; Mertens F; Rydholm A; Brosjö O; Dictor M; Mitelman F; Mandahl N
Cytogenetic analysis of four angiosarcomas from deep and superficial soft tissue.
Cancer genetics and cytogenetics 1998;100(1):52-6.
1998: Broberg K; Höglund M; Lindstrand A; Toksvig-Larsen S; Mandahl N; Mertens F
Polyclonal expansion of cells with trisomy 7 in synovia from patients with osteoarthritis.
Cytogenetics and cell genetics 1998;83(1-2):30-4.
1997: Broberg K; Limon J; Pålsson E; Lindstrand A; Toksvig-Larsen S; Mandahl N; Mertens F
Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis.
Human genetics 1997;101(3):295-8.
1997: Adeyinka A; Pandis N; Bardi G; Bonaldi L; Mertens F; Mitelman F; Heim S
A subgroup of breast carcinomas is cytogenetically characterized by trisomy 12.
Cancer genetics and cytogenetics 1997;97(2):119-21.
1997: Panagopoulos I; Thelin S; Mertens F; Mitelman F; Aman P
Variable FHIT transcripts in non-neoplastic tissues.
Genes, chromosomes & cancer 1997;19(4):215-9.
1997: Mertens F; Johansson B; Höglund M; Mitelman F
Chromosomal imbalance maps of malignant solid tumors: a cytogenetic survey of 3185 neoplasms.
Cancer research 1997;57(13):2765-80.
1997: Mitelman F; Johansson B; Mandahl N; Mertens F
Clinical significance of cytogenetic findings in solid tumors.
Cancer genetics and cytogenetics 1997;95(1):1-8.
1997: Mitelman F; Mertens F; Johansson B
A breakpoint map of recurrent chromosomal rearrangements in human neoplasia.
Nature genetics 1997;15 Spec No():417-74.
1997: Jin C; Jin Y; Wennerberg J; Akervall J; Dictor M; Mandahl N; Heim S; Mitelman F; Mertens F
Cytogenetic analysis of inverted nasal papillomas and demonstration of genetic convergence during in vitro passaging.
International journal of cancer. Journal international du cancer 1997;70(6):668-73.
1997: Jin C; Jin Y; Wennerberg J; Akervall J; Grenthe B; Mandahl N; Heim S; Mitelman F; Mertens F
Clonal chromosome aberrations accumulate with age in upper aerodigestive tract mucosa.
Mutation research 1997;374(1):63-72.
1997: Petersson C; Pandis N; Rizou H; Mertens F; Dietrich C U; Adeyinka A; Idvall I; Bondeson L; Georgiou G; Ingvar C; Heim S; Mitelman F
Karyotypic abnormalities in fibroadenomas of the breast.
International journal of cancer. Journal international du cancer 1997;70(3):282-6.
1997: Akervall J A; Michalides R J; Mineta H; Balm A; Borg A; Dictor M R; Jin Y; Loftus B; Mertens F; Wennerberg J P
Amplification of cyclin D1 in squamous cell carcinoma of the head and neck and the prognostic value of chromosomal abnormalities and cyclin D1 overexpression.
Cancer 1997;79(2):380-9.
1997: Choong P F; Rydholm A; Mertens F; Mandahl N
Musculoskeletal oncology--advances in cytogenetics and molecular genetics and their clinical implications.
Acta oncologica (Stockholm, Sweden) 1997;36(3):245-54.
1996: Mertens F; Pålsson E; Lindstrand A; Toksvig-Larsen S; Knuutila S; Larramendy M L; el-Rifai W; Limon J; Mitelman F; Mandahl N
Evidence of somatic mutations in osteoarthritis.
Human genetics 1996;98(6):651-6.
1996: Mertens F; Johansson B; Mitelman F
Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes.
Cancer genetics and cytogenetics 1996;92(1):8-10.
1996: Panagopoulos I; Pandis N; Thelin S; Petersson C; Mertens F; Borg A; Kristoffersson U; Mitelman F; Aman P
The FHIT and PTPRG genes are deleted in benign proliferative breast disease associated with familial breast cancer and cytogenetic rearrangements of chromosome band 3p14.
Cancer research 1996;56(21):4871-5.
1996: Panagopoulos I; Aman P; Mertens F; Mandahl N; Rydholm A; Bauer H F; Mitelman F
Genomic PCR detects tumor cells in peripheral blood from patients with myxoid liposarcoma.
Genes, chromosomes & cancer 1996;17(2):102-7.
1996: Lothe R A; Karhu R; Mandahl N; Mertens F; Saeter G; Heim S; Borresen-Dale A L; Kallioniemi O P
Gain of 17q24-qter detected by comparative genomic hybridization in malignant tumors from patients with von Recklinghausen's neurofibromatosis.
Cancer research 1996;56(20):4778-81.
1996: Rosai J; Akerman M; Dal Cin P; DeWever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Van de Ven W; Vanni R; Willen H
Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group).
The American journal of surgical pathology 1996;20(10):1182-9.
1996: Mandahl N; Akerman M; Aman P; Dal Cin P; De Wever I; Fletcher C D; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; Van den Berghe H; Van de Ven W; Vanni R; Willén H
Duplication of chromosome segment 12q15-24 is associated with atypical lipomatous tumors: a report of the CHAMP collaborative study group. CHromosomes And MorPhology.
International journal of cancer. Journal international du cancer 1996;67(5):632-5.
1996: Tallini G; Akerman M; Dal Cin P; De Wever I; Fletcher C D; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Van den Berghe H; Van den Ven W; Vanni R; Willen H
Combined morphologic and karyotypic study of 28 myxoid liposarcomas. Implications for a revised morphologic typing, (a report from the CHAMP Group).
The American journal of surgical pathology 1996;20(9):1047-55.
1996: Petersson C; Pandis N; Mertens F; Adeyinka A; Ingvar C; Ringberg A; Idvall I; Bondeson L; Borg A; Olsson H; Kristoffersson U; Mitelman F
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families.
Genes, chromosomes & cancer 1996;16(3):185-8.
1996: Johansson B; Mertens F; Mitelman F
Primary vs. secondary neoplasia-associated chromosomal abnormalities--balanced rearrangements vs. genomic imbalances?
Genes, chromosomes & cancer 1996;16(3):155-63.
1996: Akerman M; Dreinhöfer K; Rydholm A; Willén H; Mertens F; Mitelman F; Mandahl N
Cytogenetic studies on fine-needle aspiration samples from osteosarcoma and Ewing's sarcoma.
Diagnostic cytopathology 1996;15(1):17-22.
1996: Mertens F; Jonsson K; Willén H; Rydholm A; Kreicbergs A; Eriksson L; Olsson-Sandin G; Mitelman F; Mandahl N
Chromosome rearrangements in synovial chondromatous lesions.
British journal of cancer 1996;74(2):251-4.
1996: Choong P F; Mandahl N; Mertens F; Willén H; Alvegård T; Kreicbergs A; Mitelman F; Rydholm A
19p+ marker chromosome correlates with relapse in malignant fibrous histiocytoma.
Genes, chromosomes & cancer 1996;16(2):88-93.
1996: Akerman M; Willén H; Carlén B; Mandahl N; Mertens F
Fine needle aspiration (FNA) of synovial sarcoma--a comparative histological-cytological study of 15 cases, including immunohistochemical, electron microscopic and cytogenetic examination and DNA-ploidy analysis.
Cytopathology : official journal of the British Society for Clinical Cytology 1996;7(3):187-200.
1996: Adeyinka A; Pandis N; Nilsson J; Idvall I; Mertens F; Petersson C; Heim S; Mitelman F
Different cytogenetic patterns in skeletal breast cancer metastases.
Genes, chromosomes & cancer 1996;16(1):72-4.
1996: Pandis N; Idvall I; Bardi G; Jin Y; Gorunova L; Mertens F; Olsson H; Ingvar C; Beroukas K; Mitelman F; Heim S
Correlation between karyotypic pattern and clincopathologic features in 125 breast cancer cases.
International journal of cancer. Journal international du cancer 1996;66(2):191-6.
1996: Jin Y; Mertens F; Jin C; Wennerberg J; Mandahl N; Heim S; Mitelman F
Clonal chromosome abnormalities in two chemodectomas.
Genes, chromosomes & cancer 1996;15(3):178-81.
1996: Panagopoulos I; Höglund M; Mertens F; Mandahl N; Mitelman F; Aman P
Fusion of the EWS and CHOP genes in myxoid liposarcoma.
Oncogene 1996;12(3):489-94.
1996: Fletcher C D; Akerman M; Dal Cin P; de Wever I; Mandahl N; Mertens F; Mitelman F; Rosai J; Rydholm A; Sciot R; Tallini G; van den Berghe H; van de Ven W; Vanni R; Willen H
Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
The American journal of pathology 1996;148(2):623-30.
1995: Mertens F; Willén H; Rydholm A; Brosjö O; Carlén B; Mitelman F; Mandahl N
Trisomy 20 is a primary chromosome aberration in desmoid tumors.
International journal of cancer. Journal international du cancer 1995;63(4):527-9.
1995: Johansson B; Mertens F; Mitelman F
Cytogenetic evolution patterns in non-Hodgkin's lymphoma.
Blood 1995;86(10):3905-14.
1995: Akervall J A; Jin Y; Wennerberg J P; Zätterström U K; Kjellén E; Mertens F; Willén R; Mandahl N; Heim S; Mitelman F
Chromosomal abnormalities involving 11q13 are associated with poor prognosis in patients with squamous cell carcinoma of the head and neck.
Cancer 1995;76(5):853-9.
1995: Jin Y; Mertens F; Jin C; Akervall J; Wennerberg J; Gorunova L; Mandahl N; Heim S; Mitelman F
Nonrandom chromosome abnormalities in short-term cultured primary squamous cell carcinomas of the head and neck.
Cancer research 1995;55(14):3204-10.
1995: Mertens F; Rydholm A; Bauer H F; Limon J; Nedoszytko B; Szadowska A; Willén H; Heim S; Mitelman F; Mandahl N
Cytogenetic findings in malignant peripheral nerve sheath tumors.
International journal of cancer. Journal international du cancer 1995;61(6):793-8.
1995: Mertens F; Heim S; Kullendorff C M; Donnér M; Hägerstrand I; Mitelman F; Mandahl N
Clonal karyotypic evolution in a pediatric neurofibrosarcoma.
Cancer genetics and cytogenetics 1995;81(2):135-8.
1995: Jin Y; Mertens F; Arheden K; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Karyotypic features of malignant tumors of the nasal cavity and paranasal sinuses.
International journal of cancer. Journal international du cancer 1995;60(5):637-41.
1995: Mertens F; Heim S; Mandahl N; Mitelman F; Brun A; Strömblad L G; Kullendorff C M; Donnér M
Recurrent chromosomal imbalances in choroid plexus tumors.
Cancer genetics and cytogenetics 1995;80(1):83-4.
1995: Jin Y; Mertens F; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Tetraploidization and progressive loss of 6q in a squamous cell carcinoma of the parotid gland.
Cancer genetics and cytogenetics 1995;79(2):157-9.
1995: Aspberg F; Mertens F; Bauer H C; Lindholm J; Mitelman F; Mandahl N
Near-haploidy in two malignant fibrous histiocytomas.
Cancer genetics and cytogenetics 1995;79(2):119-22.
1995: Choong P F; Willén H; Nilbert M; Mertens F; Mandahl N; Carlén B; Rydholm A
Pigmented villonodular synovitis. Monoclonality and metastasis--a case for neoplastic origin?
Acta orthopaedica Scandinavica 1995;66(1):64-8.
1994: Panagopoulos I; Mandahl N; Ron D; Höglund M; Nilbert M; Mertens F; Mitelman F; Aman P
Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12;16 translocation.
Cancer research 1994;54(24):6500-3.
1994: Mertens F; Albert A; Heim S; Lindholm J; Brosjö O; Mitelman F; Mandahl N
Clonal structural chromosome aberrations in fibrous dysplasia.
Genes, chromosomes & cancer 1994;11(4):271-2.
1994: Gorunova L; Mertens F; Mandahl N; Jonsson N; Persson B; Heim S; Mitelman F
Cytogenetic heterogeneity in a clear cell hidradenoma of the skin.
Cancer genetics and cytogenetics 1994;77(1):26-32.
1994: Mertens F; Rydholm A; Brosjö O; Willén H; Mitelman F; Mandahl N
Hibernomas are characterized by rearrangements of chromosome bands 11q13-21.
International journal of cancer. Journal international du cancer 1994;58(4):503-5.
1994: Mertens F; Johansson B; Mitelman F
Isochromosomes in neoplasia.
Genes, chromosomes & cancer 1994;10(4):221-30.
1994: Jin Y; Mertens F; Limon J; Mandahl N; Wennerberg J; Dictor M; Heim S; Mitelman F
Characteristic karyotypic features in lacrimal and salivary gland carcinomas.
British journal of cancer 1994;70(1):42-7.
1994: Mertens F; Mandahl N; Mitelman F; Heim S
Cytogenetic analysis in the examination of solid tumors in children.
Pediatric hematology and oncology 1994;11(4):361-77.
1994: Johansson B; Mertens F; Mitelman F
Secondary chromosomal abnormalities in acute leukemias.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1994;8(6):953-62.
1994: Mertens F; Kreicbergs A; Rydholm A; Willén H; Carlén B; Mitelman F; Mandahl N
Clonal chromosome aberrations in three sacral chordomas.
Cancer genetics and cytogenetics 1994;73(2):147-51.
1994: Mandahl N; Höglund M; Mertens F; Rydholm A; Willén H; Brosjö O; Mitelman F
Cytogenetic aberrations in 188 benign and borderline adipose tissue tumors.
Genes, chromosomes & cancer 1994;9(3):207-15.
1994: Mertens F; Rydholm A; Kreicbergs A; Willén H; Jonsson K; Heim S; Mitelman F; Mandahl N
Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses.
Genes, chromosomes & cancer 1994;9(1):8-12.
1994: Mandahl N; Mertens F; Willén H; Rydholm A; Brosjö O; Mitelman F
A new cytogenetic subgroup in lipomas: loss of chromosome 16 material in spindle cell and pleomorphic lipomas.
Journal of cancer research and clinical oncology 1994;120(12):707-11.
1993: Johansson B; Mertens F; Mitelman F
Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci.
Genes, chromosomes & cancer 1993;8(4):205-18.
1993: Mertens F; Johansson B; Mitelman F
Age- and gender-related heterogeneity of cancer chromosome aberrations.
Cancer genetics and cytogenetics 1993;70(1):6-11.
1993: Mertens F; Mandahl N; Orndal C; Baldetorp B; Bauer H C; Rydholm A; Wiebe T; Willén H; Akerman M; Heim S
Cytogenetic findings in 33 osteosarcomas.
International journal of cancer. Journal international du cancer 1993;55(1):44-50.
1993: Jin Y; Mertens F; Mandahl N; Heim S; Olegård C; Wennerberg J; Biörklund A; Mitelman F
Chromosome abnormalities in eighty-three head and neck squamous cell carcinomas: influence of culture conditions on karyotypic pattern.
Cancer research 1993;53(9):2140-6.
1993: Mertens F; Orndal C; Mandahl N; Heim S; Bauer H F; Rydholm A; Tufvesson A; Willén H; Mitelman F
Chromosome aberrations in tenosynovial giant cell tumors and nontumorous synovial tissue.
Genes, chromosomes & cancer 1993;6(4):212-7.
1993: Johansson B; Heim S; Mandahl N; Mertens F; Mitelman F
Trisomy 7 in nonneoplastic cells.
Genes, chromosomes & cancer 1993;6(4):199-205.
1992: Johansson B; Bardi G; Heim S; Mandahl N; Mertens F; Bak-Jensen E; Andrén-Sandberg A; Mitelman F
Nonrandom chromosomal rearrangements in pancreatic carcinomas.
Cancer 1992;69(7):1674-81.
1992: Mertens F; Jin Y; Heim S; Mandahl N; Jonsson N; Mertens O; Persson B; Salemark L; Wennerberg J; Mitelman F
Clonal structural chromosome aberrations in nonneoplastic cells of the skin and upper aerodigestive tract.
Genes, chromosomes & cancer 1992;4(3):235-40.
1991: Mertens F; Sallerfors B; Heim S; Johansson B; Kristoffersson U; Malm C; Mitelman F
Trisomy 13 as a primary chromosome aberration in acute leukemia.
Cancer genetics and cytogenetics 1991;56(1):39-44.
1991: Johansson B; Mertens F; Heim S; Kristoffersson U; Mitelman F
Cytogenetics of secondary myelodysplasia (sMDS) and acute nonlymphocytic leukemia (sANLL).
European journal of haematology 1991;47(1):17-27.
1991: Mertens F; Johansson B; Heim S; Kristoffersson U; Mitelman F
Karyotypic patterns in chronic myeloproliferative disorders: report on 74 cases and review of the literature.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(3):214-20.
1991: Mertens F; Heim S; Mandahl N; Johansson B; Mertens O; Persson B; Salemark L; Wennerberg J; Jonsson N; Mitelman F
Cytogenetic analysis of 33 basal cell carcinomas.
Cancer research 1991;51(3):954-7.
1991: Johansson B; Mertens F; Mitelman F
Geographic heterogeneity of neoplasia-associated chromosome aberrations.
Genes, chromosomes & cancer 1991;3(1):1-7.
1990: Johansson B; Mertens F; Heim S; Kristoffersson U; Mandahl N; Nilsson P G; Mitelman F
Cytogenetic findings in acute megakaryoblastic leukemia (ANLL-M7).
Cancer genetics and cytogenetics 1990;48(1):119-23.
1990: Johansson B; Mertens F; Fioretos T; Heim S; Kristoffersson U; Mandahl N; Bartram C R; Mitelman F
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(6):448-9.
1990: Mertens F; Johansson B; Heim S; Kristoffersson U; Mandahl N; Turesson I; Malm C; Othzén A; Bartram C R; Catovsky D
Trisomy 14 in atypical chronic myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(2):117-20.
1989: Heim S; Johansson B; Mertens F
Constitutional chromosome instability and cancer risk.
Mutation research 1989;221(1):39-51.
1989: Mertens F; Heim S; Mandahl N; Johansson B; Rydholm A; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Clonal chromosome aberrations in a keratoacanthoma and a basal cell papilloma.
Cancer genetics and cytogenetics 1989;39(2):227-32.
1989: Heim S; Mertens F; Jin Y S; Mandahl N; Johansson B; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Diverse chromosome abnormalities in squamous cell carcinomas of the skin.
Cancer genetics and cytogenetics 1989;39(1):69-76.
1989: Mertens F; Heim S; Jin Y S; Johansson B; Mandahl N; Biörklund A; Wennerberg J; Jonsson N; Mitelman F
Basosquamous papilloma. A benign epithelial skin tumor with multiple cytogenetic clones.
Cancer genetics and cytogenetics 1989;37(2):235-9.
1989: Johansson B; Mandahl N; Heim S; Mertens F; Andrén-Sandberg A; Mitelam F
Chromosome abnormalities in a pancreatic adenocarcinoma.
Cancer genetics and cytogenetics 1989;37(2):209-13.
1989: Mertens F; Johansson B
Frequency and distribution of N-methyl-N'-nitro-N-nitrosoguanidine (MNNG)-induced structural chromosome aberrations in fibroblasts from sarcoma and non-Hodgkin's lymphoma patients.
Mutation research 1989;210(1):63-70.
1988: Mertens F; Johansson B; Heim S; Mandahl N; Rydholm A; Mitelman F
Bands involved in primary chromosome rearrangements in sarcomas are not constitutionally liable to breakage in sarcoma patients.
Human genetics 1988;79(4):309-14.
1988: Mertens F; Johansson B; Heim S; Mandahl N; Rydholm A; Mitelman F
Normal frequency of chromosome breakage in lymphocytes from patients with musculoskeletal sarcoma.
Cancer genetics and cytogenetics 1988;33(2):299-304.
1988: Johansson B; Mertens F
Normal level of spontaneous chromosome breakage in lymphocytes from patients with non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1988;33(1):51-7.
1988: Johansson B; Mertens F; Palm L; Englesson I; Kristoffersson U
Duplication 18p with mild influence on the phenotype.
American journal of medical genetics 1988;29(4):871-4.
1988: Johansson B; Mertens F
Frequency and distribution of mitomycin C-induced structural chromosome aberrations in lymphocytes from non-Hodgkin lymphoma patients.
Cytogenetics and cell genetics 1988;48(2):79-83.

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